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Article

Rhythmic pupillary oscillation in Creutzfeldt-Jakob disease associated with the Glu/Lys mutation of prion protein codon 200.

Movement disorders : official journal of the Movement Disorder Society - 15 Jan 2010

Nagasaka Kaori, Ohta Emiko, Nagasaka Takamura, Togashi Shinji, Miwa Michiaki, Nakamura Yuki, Shindo Kazumasa, Shiozawa Zenji

Abstract excerpt

We report two Creutzfeldt-Jakob disease (CJD) patients with rhythmic pupillary and palpebral oscillation who had a mutation of prion protein codon 200 that resulted in the substitution of lysine for glutamate (Glu/Lys). Alternating dilation and constriction of the pupils combined with elevation a...

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Identifiers

PMID: 20077484
DOI: 10.1002/mds.22884

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20077484-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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